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Modulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease
Lifestyle factors, including diet and physical activity (PA), are known beneficial strategies to prevent and delay Alzheimer’s disease (AD) development. Recently, microRNAs have emerged as potential biomarkers in multiple diseases, including AD. The aim of this review was to analyze the available in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10490103/ https://www.ncbi.nlm.nih.gov/pubmed/37686720 http://dx.doi.org/10.3390/nu15173688 |
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author | Pinto-Hernandez, Paola Castilla-Silgado, Juan Coto-Vilcapoma, Almudena Fernández-Sanjurjo, Manuel Fernández-García, Benjamín Tomás-Zapico, Cristina Iglesias-Gutiérrez, Eduardo |
author_facet | Pinto-Hernandez, Paola Castilla-Silgado, Juan Coto-Vilcapoma, Almudena Fernández-Sanjurjo, Manuel Fernández-García, Benjamín Tomás-Zapico, Cristina Iglesias-Gutiérrez, Eduardo |
author_sort | Pinto-Hernandez, Paola |
collection | PubMed |
description | Lifestyle factors, including diet and physical activity (PA), are known beneficial strategies to prevent and delay Alzheimer’s disease (AD) development. Recently, microRNAs have emerged as potential biomarkers in multiple diseases, including AD. The aim of this review was to analyze the available information on the modulatory effect of lifestyle on microRNA expression in AD. Few studies have addressed this question, leaving important gaps and limitations: (1) in human studies, only circulating microRNAs were analyzed; (2) in mice studies, microRNA expression was only analyzed in brain tissue; (3) a limited number of microRNAs was analyzed; (4) no human nutritional intervention studies were conducted; and (5) PA interventions in humans and mice were poorly detailed and only included aerobic training. Despite this, some conclusions could be drawn. Circulating levels of let-7g-5p, miR-107, and miR-144-3p were associated with overall diet quality in mild cognitive impairment patients. In silico analysis showed that these microRNAs are implicated in synapse formation, microglia activation, amyloid beta accumulation, and pro-inflammatory pathways, the latter also being targeted by miR-129-5p and miR-192-5p, whose circulating levels are modified by PA in AD patients. PA also modifies miR-132, miR-15b-5p, miR-148b-3p, and miR-130a-5p expression in mice brains, which targets are related to the regulation of neuronal activity, ageing, and pro-inflammatory pathways. This supports the need to further explore lifestyle-related miRNA changes in AD, both as biomarkers and therapeutic targets. |
format | Online Article Text |
id | pubmed-10490103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104901032023-09-09 Modulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease Pinto-Hernandez, Paola Castilla-Silgado, Juan Coto-Vilcapoma, Almudena Fernández-Sanjurjo, Manuel Fernández-García, Benjamín Tomás-Zapico, Cristina Iglesias-Gutiérrez, Eduardo Nutrients Review Lifestyle factors, including diet and physical activity (PA), are known beneficial strategies to prevent and delay Alzheimer’s disease (AD) development. Recently, microRNAs have emerged as potential biomarkers in multiple diseases, including AD. The aim of this review was to analyze the available information on the modulatory effect of lifestyle on microRNA expression in AD. Few studies have addressed this question, leaving important gaps and limitations: (1) in human studies, only circulating microRNAs were analyzed; (2) in mice studies, microRNA expression was only analyzed in brain tissue; (3) a limited number of microRNAs was analyzed; (4) no human nutritional intervention studies were conducted; and (5) PA interventions in humans and mice were poorly detailed and only included aerobic training. Despite this, some conclusions could be drawn. Circulating levels of let-7g-5p, miR-107, and miR-144-3p were associated with overall diet quality in mild cognitive impairment patients. In silico analysis showed that these microRNAs are implicated in synapse formation, microglia activation, amyloid beta accumulation, and pro-inflammatory pathways, the latter also being targeted by miR-129-5p and miR-192-5p, whose circulating levels are modified by PA in AD patients. PA also modifies miR-132, miR-15b-5p, miR-148b-3p, and miR-130a-5p expression in mice brains, which targets are related to the regulation of neuronal activity, ageing, and pro-inflammatory pathways. This supports the need to further explore lifestyle-related miRNA changes in AD, both as biomarkers and therapeutic targets. MDPI 2023-08-23 /pmc/articles/PMC10490103/ /pubmed/37686720 http://dx.doi.org/10.3390/nu15173688 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Pinto-Hernandez, Paola Castilla-Silgado, Juan Coto-Vilcapoma, Almudena Fernández-Sanjurjo, Manuel Fernández-García, Benjamín Tomás-Zapico, Cristina Iglesias-Gutiérrez, Eduardo Modulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease |
title | Modulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease |
title_full | Modulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease |
title_fullStr | Modulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease |
title_full_unstemmed | Modulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease |
title_short | Modulation of microRNAs through Lifestyle Changes in Alzheimer’s Disease |
title_sort | modulation of micrornas through lifestyle changes in alzheimer’s disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10490103/ https://www.ncbi.nlm.nih.gov/pubmed/37686720 http://dx.doi.org/10.3390/nu15173688 |
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